"Carbonic Anhydrases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A family of zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide. They play an important role in the transport of CARBON DIOXIDE from the tissues to the LUNG. EC 4.2.1.1.
Descriptor ID |
D002256
|
MeSH Number(s) |
D08.811.520.241.300.150
|
Concept/Terms |
Carbonic Anhydrases- Carbonic Anhydrases
- Anhydrases, Carbonic
- Carbonic Anhydrase
- Carbonate Dehydratase
- Dehydratase, Carbonate
|
Below are MeSH descriptors whose meaning is more general than "Carbonic Anhydrases".
Below are MeSH descriptors whose meaning is more specific than "Carbonic Anhydrases".
This graph shows the total number of publications written about "Carbonic Anhydrases" by people in this website by year, and whether "Carbonic Anhydrases" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 1 | 1 |
1998 | 1 | 0 | 1 |
1999 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2001 | 5 | 0 | 5 |
2002 | 1 | 1 | 2 |
2003 | 2 | 1 | 3 |
2004 | 1 | 0 | 1 |
2006 | 1 | 1 | 2 |
2009 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 1 | 2 |
2016 | 1 | 1 | 2 |
2017 | 1 | 1 | 2 |
2018 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Carbonic Anhydrases" by people in Profiles.
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Discovery of Potent Carbonic Anhydrase Inhibitors as Effective Anticonvulsant Agents: Drug Design, Synthesis, and In Vitro and In Vivo Investigations. J Med Chem. 2021 03 25; 64(6):3100-3114.
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Discovery of potent anti-convulsant carbonic anhydrase inhibitors: Design, synthesis, in?vitro and in?vivo appraisal. Eur J Med Chem. 2018 Aug 05; 156:430-443.
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Variants in Chemosensory Genes Are Associated with Picky Eating Behavior in Preschool-Age Children. J Nutrigenet Nutrigenomics. 2017; 10(3-4):84-92.
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Discovery of Benzenesulfonamides with Potent Human Carbonic Anhydrase Inhibitory and Effective Anticonvulsant Action: Design, Synthesis, and Pharmacological Assessment. J Med Chem. 2017 03 23; 60(6):2456-2469.
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Design and Comparative Evaluation of the Anticonvulsant Profile, Carbonic-Anhydrate Inhibition and Teratogenicity of Novel Carbamate Derivatives of Branched Aliphatic Carboxylic Acids with 4-Aminobenzensulfonamide. Neurochem Res. 2017 Jul; 42(7):1972-1982.
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Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors. J Enzyme Inhib Med Chem. 2016; 31(sup2):174-179.
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Design and synthesis of a novel class of carbonic anhydrase-IX inhibitor 1-(3-(phenyl/4-fluorophenyl)-7-imino-3H-[1,2,3]triazolo[4,5d]pyrimidin 6(7H)yl)urea. J Mol Graph Model. 2016 Mar; 64:101-109.
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High expression of carbonic anhydrase IX is significantly associated with glandular lesions in gastroesophageal junction and with tumorigenesis markers BMI1, MCM4 and MCM7. BMC Gastroenterol. 2015 Jul 09; 15:80.
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Phase I/II study of the hypoxia-activated prodrug PR104 in refractory/relapsed acute myeloid leukemia and acute lymphoblastic leukemia. Haematologica. 2015 Jul; 100(7):927-34.
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Membrane carbonic anhydrase IX expression and relapse risk in resected stage I-II non-small-cell lung cancer. J Thorac Oncol. 2014 May; 9(5):675-84.